7X8B
Crystal structure of ENL T1 mutant YEATS domain in complex with histone H3 acetylation at K27
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL02U1 |
| Synchrotron site | SSRF |
| Beamline | BL02U1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2021-07-10 |
| Detector | MAR CCD 130 mm |
| Wavelength(s) | 0.9792 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 156.732, 48.670, 47.654 |
| Unit cell angles | 90.00, 101.17, 90.00 |
Refinement procedure
| Resolution | 17.330 - 2.300 |
| R-factor | 0.1898 |
| Rwork | 0.188 |
| R-free | 0.22600 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5j9s |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | MOLREP |
| Refinement software | PHENIX (1.17.1_3660) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 30.000 | 30.000 | 2.340 |
| High resolution limit [Å] | 2.300 | 6.230 | 2.300 |
| Rmerge | 0.091 | 0.053 | 0.333 |
| Rmeas | 0.102 | 0.060 | 0.368 |
| Rpim | 0.045 | 0.027 | 0.155 |
| Total number of observations | 80119 | ||
| Number of reflections | 15862 | 799 | 801 |
| <I/σ(I)> | 15.5 | ||
| Completeness [%] | 99.6 | 95.3 | 100 |
| Redundancy | 5.1 | 4.6 | 5.5 |
| CC(1/2) | 0.997 | 0.932 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 291 | 20 % (w/v) PEG 4000, 0.1M sodium citrate pH5.6, 20 % (v/v) 2-propanol |






